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Lau, A. M. C.

Publications and source records attributed to Lau, A. M. C..

3 recordsLinked to original sources

Foldclass and Merizo-search: embedding-based deep learning tools for protein domain segmentation, fold recognition and comparison

The availability of very large numbers of protein structures from accurate computational methods poses new challenges in storing, searching and detecting relationships between these structures. In particular, the new-found abundance of multi-domain structures in the AlphaFold structure database introduces challenges for traditional structure comparison methods. We address these challenges using a fast, embedding-based structure comparison method called Foldclass which detects structural similarity between protein domains. We demonstrate the accuracy of Foldclass embeddings for homology detection. In combination with a recently developed deep learning-based automatic domain segmentation tool Merizo, we develop Merizo-search, which first segments multi-domain query structures into domains, and then searches a Foldclass embedding database to determine the top matches for each constituent domain. Combining the ability of Merizo to accurately segment complete chains into domains, and Foldclass to embed and detect similar domains, Merizo-search can be used to detect per-domain similarities for complete chains. We anticipate that these tools will enable a number of analyses using the wealth of predicted structural data now available. Foldclass and Merizo-search are available at https://github.com/psipred/merizo_search. Merizo-search is also available on the PSIPRED web server at http://bioinf.cs.ucl.ac.uk/psipred.

bioinformatics↗

Exploring structural diversity across the protein universe with The Encyclopedia of Domains

The AlphaFold Protein Structure Database (AFDB) contains full-length predictions of the three-dimensional structures of almost every protein in UniProt. Because protein function is closely linked to structure, the AFDB is poised to revolutionise our understanding of biology, evolution and more. Protein structures are composed of domains, independently folding units that can be found in multiple structural contexts and functional roles. The AFDBs potential remains untapped due to the difficulty of characterising 200 million structures. Here we present The Encyclopedia of Domains or TED, which combines state-of-the-art deep learning-based domain parsing and structure comparison algorithms to segment and classify domains across the whole AFDB. TED describes over 370 million domains, over 100 million more than detectable by sequence-based methods. Nearly 80% of TED domains share similarities to known superfamilies in CATH, greatly expanding the set of known protein structural domains. We uncover over 10,000 previously unseen structural interactions between superfamilies, expand domain coverage to over 1 million taxa, and unveil thousands of architectures and folds across the unexplored continuum of protein fold space. We expect TED to be a valuable resource that provides a functional interface to the AFDB, empowering it to be useful for a multitude of downstream analyses.

bioinformatics↗

Deuteros: software for rapid analysis and visualization of data from differential hydrogen deuterium exchange-mass spectrometry

SummaryHydrogen deuterium exchange-mass spectrometry (HDX-MS) has emerged as a powerful technique for interrogating the conformational dynamics of proteins and their complexes. Currently, analysis of HDX-MS data remains a laborious procedure, mainly due to the lack of streamlined software to process the large datasets. We present Deuteros which is a standalone software designed to be coupled with Waters DynamX HDX data analysis software, allowing the rapid analysis and visualization of data from differential HDX-MS.\n\nAvailabilityDeuteros is open-source and can be downloaded from https://github.com/andymlau/Deuteros, under the Apache 2.0 license.\n\nImplementationwritten in MATLAB and supported on both Windows and MacOS. Requires the MATLAB runtime library.\n\nContactargyris.politis@kcl.ac.uk

bioinformatics↗